NDC 55111-194

NDC 55111-194

NDC 55111-194 is a in the category. It is labeled and distributed by .

Proprietary NameNDC 55111-194
Marketing Category/

Packaging

NDC SPL Data Element Entries

NDC 55111-194-30 [55111019430]

Fexofenadine Hydrochloride TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA076502
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2006-04-12
Marketing End Date2011-01-25

NDC 55111-194-01 [55111019401]

Fexofenadine Hydrochloride TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA076502
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2006-04-12
Marketing End Date2011-01-25

NDC 55111-194-90 [55111019490]

Fexofenadine Hydrochloride TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA076502
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2006-04-12
Marketing End Date2011-01-25

NDC 55111-194-78 [55111019478]

Fexofenadine Hydrochloride TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA076502
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2006-04-12
Marketing End Date2011-01-25

NDC 55111-194-05 [55111019405]

Fexofenadine Hydrochloride TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA076502
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2006-04-12
Marketing End Date2011-01-25

NDC 55111-194-89 [55111019489]

Fexofenadine Hydrochloride TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA076502
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2011-01-25
Marketing End Date2011-01-25

NDC 55111-194-79 [55111019479]

Fexofenadine Hydrochloride TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA076502
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2006-04-12
Marketing End Date2011-01-25

Drug Details

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